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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036246Generated: November 3, 2026

Benzyloxycarbonylglycine → HCID 66654564, compound

https://huagongshe.com/reaction/2036246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxycarbonylglycineHCID 14349—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 66654555HCID 66654555—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66654564HCID 66654564—

Reaction Steps

A solution of N-carbobenzyloxyglycine (1.07 g, 5.00 mmol, 1.0 eq.) and (±)-[4-fluoro-2-(1,2,3,4-tetrahydro-isoquinolin-1-yl)-phenoxy]-acetic acid ethyl ester hydrochloride (1.93 g, 5.00 mmol, 1.0 eq.) in DMF (30 mL) was treated with 4-(dimethylamino)pyridine (2.44 g, 20.00 mmol, 4.0 eq.) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1.44 g, 7.50 mmol, 1.5 eq.) and the resulting solution was stirred at r.t. for 18 hours. The reaction mixture was diluted with AcOEt (500 mL). The diluted solution was washed with 1N aq. HCl soln. (3×200 mL), sat. aq. NaHCO3 soln. (3×200 mL), sat. aq. NaCl soln. (1×200 mL), dried over MgSO4, and concentrated in vacuo. The crude product was purified by flash master (column: 100 g, flow: 35 mL/min, heptane to heptane+AcOEt) to yield the title product as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575158B2
Source datasetuspto-grants-2013_11
ORD IDord-cf3d6bb6ab224891a0214985c3fa6816
Source noteuspto-grants-2013_11